ClinVar Miner

Variants in gene ANKRD1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 5
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NM_014391.2(ANKRD1):c.346-15_346-14del rs794728971
NM_014391.2(ANKRD1):c.346-17_346-10del rs397517250
NM_014391.2(ANKRD1):c.346-29_346-12del rs72003210
NM_014391.3(ANKRD1):c.417C>A (p.Phe139Leu) rs201398260
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val) rs35550482

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